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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734574Generated: October 26, 2026

Methanesulfonyl chloride → 2-[3-(2-Oxo-1,3-oxazolidin-3-yl)phenyl]ethyl methanesulfonate

https://huagongshe.com/reaction/734574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-[3-(2-Hydroxyethyl)phenyl]-1,3-oxazolidin-2-oneHCID 54243811—
Product2-[3-(2-Oxo-1,3-oxazolidin-3-yl)phenyl]ethyl methanesulfonateHCID 5744434093%

Reaction Steps

The title compound was prepared in 93% yield according to the general procedure for the preparation of amides (Method B) starting from starting from 3-[3-(2-hydroxyethyl)phenyl]-1,3-oxazolidin-2-one and methanesulfonyl chloride. The crude material was purified on SPE cartridge (Silica) using as eluent a gradient from cyclohexane (100%) to cyclohexane-ethyl acetate (8:2) affording the final compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592346B2
Source datasetuspto-grants-2009_09
ORD IDord-575feae8f8ee43f382badc3150f8d679
Source noteuspto-grants-2009_09